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Erschienen in: Journal of Nuclear Cardiology 3/2021

Open Access 11.05.2020 | TECHNICAL CORNER

Technical aspects of gated SPECT MPI assessment of left ventricular dyssynchrony used in the VISION-CRT study

verfasst von: Amelia Jimenez-Heffernan, MD, PhD, FEBNM, FASNC, Sadaf Butt, MD, Claudio T. Mesquita, MD, Teresa Massardo, MD, Amalia Peix, MD, PhD, FACC, FASNC, Alka Kumar, MD, Chetan Patel, MD, Erick Alexanderson, MD, FACC, Luz M. Pabon, MD, Ganesan Karthikeyan, MD, MSc, Claudia Gutierrez, MD, Victor Marin, MD, Ernest Garcia, PhD, Diana Paez, MD, MSc

Erschienen in: Journal of Nuclear Cardiology | Ausgabe 3/2021

Hinweise

Electronic supplementary material

The online version of this article (https://​doi.​org/​10.​1007/​s12350-020-02122-3) contains supplementary material, which is available to authorized users.
The authors of this article have provided a PowerPoint file, available for download at SpringerLink, which summarises the contents of the paper and is free for re-use at meetings and presentations. Search for the article DOI on SpringerLink.com.
The authors have also provided an audio summary of the article, which is available to download as ESM, or to listen to via the JNC/ASNC Podcast.

Funding

IAEA Coordinated Research Protocol E1.30.34 funded the VISION-CRT trial.

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Abkürzungen
CRT
Cardiac resynchronization therapy
ECTb4
Emory Cardiac Toolbox version 4
ES
End systole
ED
End diastole
LBBB
Left bundle branch block
LVdys
Left ventricular mechanical dyssynchrony
LVEF
Left ventricular ejection fraction
gMPI
Gated myocardial perfusion imaging
PSD
Phase standard deviation

Introduction

Clinical interest continues in identifying heart failure patients who will improve with cardiac resynchronization therapy (CRT). Since the advent of applying phase analysis to measure the synchronicity of the regional LV onset of mechanical contraction1 and the availability, automation and reproducibility of measuring phase from gated SPECT MPI (gMPI) associated with this process there has been a need to properly evaluate this methodology. This need prompted the International Atomic Energy Agency (IAEA) to fund a multicenter trial to study this opportunity. The trial was titled ‘‘Value of intraventricular synchronism assessment by gated SPECT myocardial perfusion imaging in the management of heart failure patients submitted to cardiac resynchronization therapy’’ (IAEA VISION-CRT). Several reports on the findings of this trial are already published24 and other reports are forthcoming.
The purpose of this report is to describe the technical considerations undertaken in this trial to assure valid results and the algorithms in ECTb4 used to measure synchronicity-pertinent LV parameters. Some of the descriptions below are specific to using ECTb4. The quality control, the processing technical tips and algorithms descriptions are universal to technologists, physicians and industries interested in assessing LV mechanical dyssynchrony (LVdys).

Technical Aspects of gMPI Acquisition and Reconstruction

Acquisition

The SPECT scans are performed approximately 30 minutes post rest injection using 740-1110 MBq (20-30 mCi) of 99mTc-sestamibi or tetrofosmin. SPECT images are usually acquired on dual-headed cameras with high-resolution low energy collimators, using 180° orbits and a standard resting protocol.
Gating errors can cause errors in the measurement of LV dyssynchrony,5 usually seen in patients with atrial fibrillation or ectopic beats. These may result in a reduction of counts in the late frames and are typically detected as flickering in gated short-axis (SA) and/or gated planar projection cine displays; the drop in counts has the effect of making the LVdys measurement appear more synchronous than in reality. Patients being imaged to guide CRT are required to be in sinus rhythm. Those cases experiencing arrhythmias are instrumented with conventional pacemakers to bring them to sinus rhythm before being considered for enhancement to biventricular pacing with CRT, which helps but does not totally eliminate the gating error. Because of this concern, a 100% (50%-150%) R-to-R gating window is used. Another approach is to use a narrower R-to-R window such as 40% (80%-120%) R-to-R. This approach works best in systems where the acquisition per projection can be constrained to a preset number of myocardial counts per projection, otherwise projections with more rejected beats would have less counts and can create reconstruction artifacts.
Either 8 or 16 frames per cardiac cycle are used for ECG gating. Since the measurement of phase is count sensitive, i.e., the more counts the more accurate the dyssynchrony measurement, the choice of number of frames is dictated by the number of counts per pixel in the gated LV myocardium (see Table 1). Thus, if all variables are the same except 8 or 16 frames, the myocardial pixels from the 8 frame gated study will have twice the counts as the 16 frames study, and although counter-intuitive will yield a more accurate determination of LV dyssynchrony. Temporal resolution of phase analysis is related to count density per myocardial pixel and has been shown to be 5.6° corresponding to 1/64 of the cardiac cycle in common clinical acquisitions using gated SPECT with 8 or 16 frames per cardiac cycle. Both the accuracy of the ECG gating as well as the appropriateness of the count density are monitored using specialized QC algorithms shown in Figure 1.
Table 1
Technical quality recommended for the accurate measurement of LV dyssynchrony from SPECT gMPI studies
Technical Quality
Max Counts in Gated LV
Adequate
> 80 (300 typical)
Marginal
20–80
Inadequate
< 20

Reconstruction and Filtering

All images are reconstructed in the standard way using OSEM with 3 iterations and 10 subsets and filtered by a Butterworth filter, power 10, using a cut-off frequency of 0.3 cycles/mm. Although there are reports that the reconstruction approach does not have a strong impact on the LVdys calculation the goal is to optimizing the number of counts per pixel. Reconstructed trans-axial images are reoriented into SA slices used conventional methods.
Additional spatial-temporal filtering is performed on the reconstructed gated SA slices to reduce count noise. A 3 × 3 × 3 121/242/121 3D filter is first applied. A second adaptive filter is applied when a pixel located in the myocardium changes ≤ 5 counts between systole and diastole. This triggers that the counts in the pixel be replaced by the weighted average of its 8 2D neighbors.

gMPI Processing and Quantification

The relatively linear relationship between myocardial thickening and myocardial count density in all segments is the basis for the assessment of LV dyssynchrony by phase analysis. Thickening is measured from the change in LV myocardial pixel counts from systole to diastole. Therefore, the time-activity curve of a myocardial segment is equivalent to its temporal thickening curve. A first-harmonic Fourier transformation is used to replace the discrete counts from each time-activity curve by a continuous thickening curve with good temporal resolution. The onset of myocardial contraction is then obtained from the crossing of the thickening curve with a line representing the average thickening for the curve.1,6 Both the measurements of thickening and onset of contraction measurements have been shown to be robust even in areas of hypoperfused myocardium allowing a good differentiation of patients with cardiac dysfunction from normal ones.6

Processing Quality Control

Careful processing of gated SPECT MPI for dyssynchrony assessment is required to avoid and guarantee consistency. Therefore, a systematic approach is needed for optimal phase analysis.7 Automatic determination of gated center, radial extent and apex is robust, repeatable, and consistent with conventional processing. As always, operators are required to confirm that the algorithm correctly detected these landmarks and correct them manually if needed.
It is the base definition, the valve plane that carries the main error in both automatic and manual parameters creation.7 Automatic software may not be optimized for locating the gated valve plane for the precision required for phase analysis and thus the user must make sure processing parameters are appropriate.
When processing with ECTb, a correctly automatically detected LV base SA slice should look like a backwards C and the apex should look like a cap without a hole in it (Figure 2). This is true for both the ungated as well as the gated SA slices. This algorithm has been enhanced to emphasize accuracy in measuring LV dyssynchrony algorithm by starting with the base and apex detection from the ungated images as a starting point for iterative processing of gated parameters. Next, the base and apex selection from the ungated images are used in the ES gated image. In the subsequent gated images from ES to ED the base selection is moved outward depending on the patient’s initial LVEF as follows:
(1)
if the LVEF > 50% the base is allowed to move 2 slices in from ES to ED;
 
(2)
if the LVEF > 35% and ≤ 50%, the base is allowed to move 1 slice from ES to ED;
 
(3)
if the LVEF ≤ 35%, the base selection is not allowed to move.
 
These base selections can then be used to recalculate LVEF and repeat the base selection process until the described below are reduced or eliminated.
This base selection is designed to reduce created errors by including pixels from non-contracting regions that produce false areas of dyssynchrony in the phase map, usually at the base, and for the abnormal study it can change the location and severity of existing dyssynchrony. Moreover, techniques that increase the accuracy of phase analysis also promote the accuracy of all functional parameters.

Quantification to Help Guide and Evaluate CRT

The LV functional parameters used to identify potential responders to CRT were the LVEF (< 35% by echo) and the magnitude of intraventricular dyssynchrony (PSD > 43° by ECTb48) at baseline before CRT. PSD is the standard deviation of the phase distribution (Figure 3), which was used as the preferred parameter to measure LV dyssynchrony. Note that even though the normal PSD cut-off with ECTb was measured as 24.4° for men and 22.2° for women1 it does not mean that patients that exceed this threshold are in heart failure or require CRT. Also, note that the PSDs measured by other algorithms are probably different from those by ECTb4.
The identification of the last contracting viable segment(s) by ECTb4 is used to identify the target region in the LV to place the CRT lead via venous access.9 The LV functional parameters, measured by ECTb4, used to identify improved clinical response 6 months post CRT were as follows2: an improvement in LVEF ≥ 5%, a reduction in ESV by ≥ 15% and or an improvement in LVdys SD by ≥ 4°.
LVEF and ESV were measured by ECTb4 in the conventional way. The amount of LVdys is measured as the PSD.1 Another parameter used to measure LVdys is the phase bandwidth, which is measured as the range in degrees which includes 95% of the elements in the phase histogram. The PSD parameter is preferred over the histogram bandwidth because it is less susceptible to phase noise. An example of a phase histogram from a typical patient being evaluated for CRT is shown in Figure 3.
The automatic determination of the last viable segment(s) to contract were determined as previously reported.10 Briefly, this is a three-step process (Figure 4). First, the phase polar map is divided into the 17-segment model and the average phase for each segment is determined representing the onset of mechanical contraction for that segment. Second, each pixel in the polar map of the resting perfusion distribution ≤ 50% of the maximum relative counts is identified as non-viable and the percent of non-viable pixels for each of the 17 segments is calculated as well as the percent of the total LV that is non-viable. Third, for each patient that the total LV that is non-viable is < 50%, and for only the non-apical segments that are in the anterior, anterolateral, inferolateral and inferior walls the algorithm determines the segment with the largest average phase and with the extent of viability > 50% as the last viable segment to contract. Other viable segments within 10° of the last segment are also identified in case there is no practical venous access to the last viable contracting segment.

Conclusion

This report presents helpful tips used in the VISION-CRT trial intending to explain and guide the correct gMPI acquisition, processing and parametrization of synchrony-pertinent LV functional parameters that may assist in the identification of patients who respond to CRT and in the evaluation of the treatment. The procedures described in this report were used by the nuclear cardiology core laboratory at Emory University to generate the trial’s results and each of the individual trial sites independently followed this guidance to generate the site’s results. By following these procedures applied to the automated algorithms described here should ensure widespread use of reproducible dyssynchrony measurement techniques that overcome the disagreements reported in the PROSPECT trial when using echocardiographic techniques for the same purpose.12 The agreement between the Emory core lab results and those from the independent VISION-CRT sites is the subject of a future report.

Disclosures

Dr. Ernest Garcia receives royalties from the sale of the Emory Cardiac Toolbox and has equity positions with Syntermed, Inc. The terms of these arrangements have been reviewed and approved by Emory University in accordance with its conflict of interest policies. Amelia Jimenez-Heffernan, Sadaf Butt, Claudio T Mesquita, Teresa Massardo, Amalia Peix, Alka Kumar, Chetan Patel, Erick Alexanderson, Luz M Pabon, Ganesan Karthikeyan, Claudia Gutierrez, Victor Marin, and Diana Paez have no conflicts of interest to disclose.
Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://​creativecommons.​org/​licenses/​by/​4.​0/​.

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Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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Anhänge

Electronic supplementary material

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Metadaten
Titel
Technical aspects of gated SPECT MPI assessment of left ventricular dyssynchrony used in the VISION-CRT study
verfasst von
Amelia Jimenez-Heffernan, MD, PhD, FEBNM, FASNC
Sadaf Butt, MD
Claudio T. Mesquita, MD
Teresa Massardo, MD
Amalia Peix, MD, PhD, FACC, FASNC
Alka Kumar, MD
Chetan Patel, MD
Erick Alexanderson, MD, FACC
Luz M. Pabon, MD
Ganesan Karthikeyan, MD, MSc
Claudia Gutierrez, MD
Victor Marin, MD
Ernest Garcia, PhD
Diana Paez, MD, MSc
Publikationsdatum
11.05.2020
Verlag
Springer International Publishing
Erschienen in
Journal of Nuclear Cardiology / Ausgabe 3/2021
Print ISSN: 1071-3581
Elektronische ISSN: 1532-6551
DOI
https://doi.org/10.1007/s12350-020-02122-3

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